Canonical Allele Identifier: CA2815543186
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070128_22070129insA , CM000682.2:g.22070128_22070129insA GRCh38
NC_000020.10:g.22050766_22050767insA , CM000682.1:g.22050766_22050767insA GRCh37
NC_000020.9:g.21998766_21998767insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1440_445+1441insA